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1 ecies, from fish to mammals, albeit not in a urodele.
2 he idea that they may also function in adult urodeles.
3 hanistic novelties in amniotes, anurans, and urodeles.
4 e features classically regarded as unique to urodeles.
5 ecules during the process of regeneration in urodeles.
6 d a critical control of limb regeneration in urodeles.
7                                   In certain urodeles, a lost appendage, including hand and foot, can
8 morphogenesis of superficial mesoderm in the urodeles Ambystoma maculatum, Ambystoma mexicanum, and T
9 s for a contributing factor in the deficient urodele amphibian Ab responses.
10 ribution to the peptides found in anuran and urodele amphibian orders.
11 ral nervous system of adult specimens of the urodele amphibian Pleurodeles waltl.
12  and recently metamorphosed juveniles of the urodele amphibian Pleurodeles waltl.
13 VT-immunoreactivity (ir) was greater in this urodele amphibian than in any other species.
14                                  The newt, a urodele amphibian, is able to repeatedly regenerate its
15                               The axolotl, a urodele amphibian, provides a model with all the benefit
16  distributed in specific brain areas of this urodele amphibian.
17                                              Urodele amphibians (newts and salamanders) are of partic
18                                              Urodele amphibians (salamanders) are important models fo
19                      The only exceptions are urodele amphibians (salamanders), whose limb elements de
20                                              Urodele amphibians and teleost fish regenerate amputated
21 etazoan phylogeny, but among vertebrates the urodele amphibians are exceptional.
22                                 For example, urodele amphibians can completely regenerate all lost ti
23                           Teleost fishes and urodele amphibians can regenerate amputated appendages,
24                     The regenerating limb of urodele amphibians is an important system for evaluating
25                           In contrast, adult urodele amphibians make larval-like responses and are no
26                         Tooth development in urodele amphibians occurs from a restricted region of an
27                       Adult teleost fish and urodele amphibians possess a spectacular ability to rege
28   These findings support the conclusion that urodele amphibians possess a well-developed vasotocin sy
29                                         Some urodele amphibians possess the capacity to regenerate th
30                                              Urodele amphibians regenerate appendages through the rec
31                                        Adult urodele amphibians such as the newt have remarkable rege
32 ms governing pluripotency are conserved from urodele amphibians to mammals.
33                              The capacity of urodele amphibians to regenerate a variety of body parts
34  the commonly studied vertebrate models (the urodele amphibians).
35 imitive ectoderm of embryos from mammals and urodele amphibians, and here we report the isolation of
36  extensive ability for adult regeneration as urodele amphibians, including 1 of the more popular mode
37                                           In urodele amphibians, lens induction during development an
38                    We show here that, in two urodele amphibians, newts and axolotls, the regulation o
39 ation in embryos from axolotls, representing urodele amphibians, since urodele embryology is basal to
40                                           In urodele amphibians, the hypothalamic neuropeptide argini
41 is a property that seems to be restricted to urodele amphibians.
42 ief regenerators, including teleost fish and urodele amphibians.
43 ue expansions in mTOR protein sequence among urodele amphibians.
44  of limb loss and limb re-evolution, and the urodele and caecilian in our sample.
45 te susceptibility and disease progression in urodeles and determine differences in pathogenicity betw
46                                              Urodeles and fetal mammals are capable of impressive epi
47 cuments the morphological diversity of early urodeles and includes larvae and adults of both neotenic
48 idate the mechanisms of lens regeneration in urodeles and its absence in higher vertebrates.
49 e difference in regenerative ability between urodeles and mammals.
50  the restorative trajectory observed in some urodeles and teleosts, resulting in the formation of a s
51             During appendage regeneration in urodeles and teleosts, tissue replacement is precisely r
52       With ten extant families, salamanders (urodeles) are one of the three major groups of modern am
53                                              Urodeles begin gastrulation with much of their presumpti
54 issues within a body and among species, with urodeles being the most spectacular.
55 ally be used to identify subdivisions in the urodele brain similar to other vertebrates, which are no
56 due to the generally pedomorphic features of urodele brains.
57  this taxon, pushing back the rock record of urodeles by at least 60 to 74 Ma (Carnian-Bathonian).
58                                        Adult urodeles can regenerate their limbs by local formation o
59 ly discovered differential responsiveness of urodele cells to factors present in serum at the wound s
60 lly, Pax6 is broadly expressed all along the urodele CNS (olfactory bulbs, pallium, basal ganglia, di
61 ralized model for tetrapod limb development, urodeles deviate from anurans and amniotes in at least t
62 otls, representing urodele amphibians, since urodele embryology is basal to amphibians and was conser
63 o theories of sperm competition because most urodele females--in contrast to other vertebrate females
64        Subduction may be a common feature of urodele gastrulation, differing in this regard from anur
65  is widely maintained in the brains of adult urodeles, in contrast to the situation in other tetrapod
66 ment proteins in regenerative tissues of the urodele lens and limb supports a nonimmunologic function
67 sion and the effects of exogenous FGF during urodele lens regeneration were conserved.
68                    Following amputation of a urodele limb or teleost fin, the formation of a blastema
69 e target genes regulated by retinoic acid in urodele limb regeneration, we have used pseudotyped retr
70  expressed in the regenerating tissue during urodele limb regeneration.
71 placed through regeneration (for example, in urodeles, lizards, arthropods and crustaceans) or perman
72                                          The urodele myotube responds to a ligand generated downstrea
73                   Anuran (frog) tadpoles and urodeles (newts and salamanders) are the only vertebrate
74         The molecular pathway(s) involved in urodele regeneration are largely unknown.
75 s we understand more about the mechanisms of urodele regeneration.
76                        Among tetrapods, only urodele salamanders, such as the axolotl Ambystoma mexic
77                                              Urodeles (salamanders) are able to completely regenerate
78                                        Adult urodeles (salamanders) are unique in their ability to re
79                                        Adult urodeles (salamanders) are unique in their ability to re
80 s in both cartilaginous fishes (dogfish) and urodeles (salamanders), rod OFF bipolar cells and their
81 nique form of polyphenism found in dozens of urodele species worldwide, leads to the production of tw
82  be involved in limb regeneration in certain urodele species.
83 re akin to tissue renewal in mammals than to urodele tail regeneration.
84 tanding the cellular plasticity that enables urodeles to regenerate many tissues is important for det
85                   This remarkable ability of urodeles to restore entire limbs has been largely linked
86    To investigate germ cell determination in urodeles, where germ plasm has never been conclusively i